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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Zfp276tm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:7510125
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Zfp276tm1c(EUCOMM)Hmgu/Zfp276tm1c(EUCOMM)Hmgu
Tg(Sox10-cre)1Wdr/0
involves: C57BL/6 * C57BL/6N * CBA MGI:7619747


Genotype
MGI:7619747
cn1
Allelic
Composition
Zfp276tm1c(EUCOMM)Hmgu/Zfp276tm1c(EUCOMM)Hmgu
Tg(Sox10-cre)1Wdr/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Sox10-cre)1Wdr mutation (2 available)
Zfp276tm1c(EUCOMM)Hmgu mutation (0 available); any Zfp276 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice show a transient delay in oligodendrocytes (OL) maturation and myelination: cells expressing Myrf protein (an OL maturity marker) in transverse spinal cord sections are reduced to 56% of controls at P7, with similar decreases noted in cells expressing myelin genes Mbp and Plp1 and Gstpi protein; at P30 only a slight reduction in Gstpi numbers is still observed, whereas no differences in all other differentiation markers and myelin genes are detected at P30 or P60
• however, overall numbers of Sox10+ oligodendroglial cells (OGCs), Pdgfra+ oligodendrocyte progenitor cells (OPCs), Gfap+ astrocytes, and Iba1+ microglia are not significantly changed in the spinal cord at P1-P60
• cells expressing myelin genes Mbp and Plp1 and Gstpi protein are significantly reduced in transverse spinal cord sections at P7; however, only a slight reduction in Gstpi numbers is still observed at P30
• analyses of spinal cord white matter regions showed an increased g-ratio and a drastically reduced number of myelinated axons at P7 but not at P30, indicating a transient delay in the myelination of axons in early postnatal stages
• mice show strongly reduced expression of myelin genes in the spinal cord at P7
• in vitro, RNA-Seq analyses of primary OGC cultures derived from P0-P3 forebrains show significant downregulation of myelination-related genes, consistent with the delayed oligodendrocyte differentiation and hypomyelination phenotype seen in vivo

homeostasis/metabolism
• RNA-Seq analyses of primary OGC cultures derived from P0-P3 forebrains show significant downregulation of genes associated with fatty acid, cholesterol and sphingomyelin biosynthesis





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory